NDC 72059-001 Sting Relief Medicated Pad

  1. Labeler Index
  2. Nantong Sirius Packing Products Co., Ltd.
  3. NDC: 72059-001 Sting Relief Medicated Pad

NDC Product Code 72059-001

NDC CODE: 72059-001

Proprietary Name: Sting Relief Medicated Pad What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 72059 - Nantong Sirius Packing Products Co., Ltd.

NDC 72059-001-01

Package Description: 1 SWAB in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Sting Relief Medicated Pad with NDC 72059-001 is a product labeled by Nantong Sirius Packing Products Co., Ltd.. The generic name of Sting Relief Medicated Pad is . The product's dosage form is and is administered via form.

Labeler Name: Nantong Sirius Packing Products Co., Ltd.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nantong Sirius Packing Products Co., Ltd.
Labeler Code: 72059
Start Marketing Date: 02-01-2018 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Sting Relief Medicated Pad Product Label Images

Sting Relief Medicated Pad Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Medicinal Ingredient:Benzocaine6%

Purpose

Topical Anesthetic

Use

For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites

Directions

Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician.

Warnings

FOR EXTERNAL USE ONLY.FLAMMABLE,Keep away from fire or flame.Do not use in the eyes ,if contact occurs ,flush eyes with water.other information sotre at room temperature 15








OC-30








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OF)

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. if swallowed get medical help or contact a Poison Control Center right away.

Inactive Ingredients

Isopropyl alcohol,purified water

* Please review the disclaimer below.